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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10755생성일: 2026년 10월 25일

4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene → 1-Hydroxy-6-(trifluoromethyl)benzotriazole

https://huagongshe.com/reaction/10755

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
반응물Hydrazine hydrate (1:1)HCID 24654—
용매EthanolHCID 702—
생성물1-Hydroxy-6-(trifluoromethyl)benzotriazoleHCID 68819489.5%

반응 단계

The title compound is prepared according to the procedure described by K. Takeda [J. Org. Chem., 50, 273, (1985)]. A mixture of 4-chloro-3-nitro-α,α,α-trifluorotoluene (50.0 g, 0.22 moles) and hydrazine hydrate (33.0, 0.33 moles) in absolute ethanol (75 ml) is refluxed for 24 h. After removal of the solvent under reduced pressure, the residue is dissolved in 10% aqueous sodium carbonate solution. The solution is washed with ether to remove the starting material and acidified with concentrated HCl to precipitate the product, which is washed with water and dried to obtain 40.0 g of the title compound. This product is recrystallized from ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094872B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-868789ba44d24a379570d31b85128dc2
출처 메모uspto-grants-2006_08